1ml
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Ionic polarizability at a flow rate is about 1ml / min by gradient elution .
离子的极化率梯度洗脱。
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Physiological saline ( 1ml ) was injected into the knee joints of the controls .
Ⅱ组注射1ml生理盐水为对照。
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THE DEVELOPMENT OF GRIN OPTICS at a flow rate is about 1ml / min by gradient elution .
梯度折射率光学的发展现状梯度洗脱。
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The animals were injection of 3 % pentobarbital ( 1ml / mg ), then underwent surgery .
每只豚鼠给予3%戊巴比妥(1ml/kg)腹腔注射下行外科手术。
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The model of leukopenia was built by giving benzene ( s. c 1ml / kg ) to the rabbits .
家兔皮下注射苯1ml/kg,造成白细胞减少症模型。
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Under the concentration of 1ml / kg and 2ml / kg , the difference of the branch growth was not significant ;
对于新梢生长量,1ml/kg和2ml/kg浓度处理下的差异不显著;
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The treatment , developed by a French biotech company called Cellectis , consisted of 1ml of UCART19 cells injected into Layla 's bloodstream .
这一疗法是由法国生物科技公司Cellectis开发出来的,把1毫升的UCART19细胞注入了莱拉的血流中。
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In the experiment , each chicken has taken 0.5g ~ 3g such medicine mixed with feed or 1mL ~ 3mL decoction mixed with drinking water per day .
对鸡的防治试验,按毎只鸡每日0.5g~3g剂量,混饲喂服或水煎剂毎只鸡每日1-3mL剂量,混入水中饮服。
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Methods After sterilized Chinese ink ( 1ml ) was infused in normal tissue at four points , extensive cervical resection and cleaning operation of pelvic lymph nodes were performed .
方法宫颈癌周围正常组织内分4点注射中华墨汁每点1ml后,行广泛子宫切除术和盆腔淋巴清扫术。
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Methods : After anesthesia , myocardial contrast echocardiography was performed in 10 closed chest dogs by peripheral intravenous injection of Sigma contrast agent ( 1ml / kg ) .
方法:对10条闭胸犬麻醉后经周围静脉注射Sigma造影剂(1ml/kg)进行心肌声学造影。
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Rats above were treated by intragastric administration with 1ml / 100g at 8:30-10:00 everyday , while the ones in normal control group were treated with distilled water by the same volume .
正常对照组给予蒸馏水灌胃。每天8:30-10:00灌胃给药,给药容积为1ml/100g。
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The CPC solid powder and curing liquid were mixed in the port according to the proportion of2g : 1ml and get paste mixture , namely the CPC dough .
将CPC固体粉末与固化液按照2g:1ml的比例在研钵中混合均匀,得到糊状混合物,即CPC面团。
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Other groups were injected in the abdominal cavity 1mL / kg 40 % CCl4 - oil ( 2 times per week ), while oral administration , 1 time per day for 4 weeks .
除模型组外,其余各组腹腔注射的同时灌胃给药,每日1次,共4周。
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The AHNP model was induced by retrograde intraductal administration of 5 % sodium taurcholate ( 1ml / kg , 0.1ml / min ) .
模型组经胆胰管逆行注射5%牛磺胆酸钠(1ml/kg,0.1ml/min)诱发AHNP;
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SAP group : SAP was induced in male SD rats by the retrograde injection of 5 % sodium taurocholate ( 1ml / kg ) into the biliopancreatic duct .
采用4%水合氯醛(10ml/kg)腹腔注射麻醉,逆行胰胆管注射5%牛磺胆酸钠(1ml/kg)建立SAP模型。
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The quaternary ammoniation reaction conditions are confirmed by the orthogonal test . The intrinsic viscosity and the quaternary ammonium of the product are 1175 . 1mL / g and 20.1 % respectively .
通过正交实验确定了季铵化反应的最佳工艺条件,产物P(AM-AAC)的特性粘数为1175.1mL/g,季铵化度为20.1%。
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Operation group were made by injected autologous no-heparinized artery blood 1ml / kg body weight into chiasmatic cistern for the first time , once again 0.5ml/kg body weight after 48 hours ;
手术组采用开颅两次视交叉池注血法,首次按1.0ml/kg体重注入自体非肝素化血,48小时后按0.5ml/kg体重再次注血;
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The treatments were daily conducted by intragastric administration for 13 weeks based on body weight which was weighed once a week . The capacity of intragastric administration were 1ml / 100g body weight .
每周定时称量体重,每日AP灌胃染毒,根据体重计算染毒量,灌胃容量为1ml/100g体重,持续染毒13周。
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The dosage of 4 patients with bilateral masseteric hypertrophy was 50 U / 1ml for each side and the dosage of the other one with left hypertrophy was 60 U / 1ml .
其中4例双侧咬肌肥大每侧注射剂量为50U/1ml,1例单侧肥大注射剂量为60U/1ml。
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Methods : Fertilized rats were divided into three groups , 40 % iodide oil was injected into two high iodine group 's stomach through mouth with 1ml / kg . bw at day 0 and day 7 respectively .
方法:受精大鼠分成3个组,2个高碘组分别在受孕0d和7d一次性经口灌胃给予1ml/kg。
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Adult female guinea pig were randomly assigned into three groups : control ( 1ml / kg NaCl ), ischemic / reperfusion ( 1ml / kg NaCl ), Fosinopril ( 10 mg / kg ) .
雌性成年豚鼠随机分为3组:对照组(1ml/kg生理盐水),缺血再灌注组(1ml/kg生理盐水),福辛普利组(10mg/kg)。
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After 2.7 ml of heparin saline and diluted blood had been discarded , 3 blood samples ( 1ml each ) were obtained from the radial arterial pressure tube successively as A , B and C test groups .
自桡动脉测压管弃去2.7ml的肝素盐水和稀释血后,取3份血样,每份1ml,依次为A、B、C组,为实验组。
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And in animal feed to the required time , with 4 % chloral hydrate ( 1ml / 100g ) after intraperitoneal injection of anesthesia , conventional perfusion fixation , the brains were removed intact .
并在动物喂养至规定时间后,以4%水合氯醛(1ml/100g)腹腔注射麻醉后,常规灌流固定,完整取出脑组织。
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The test results have shown the critical preheat temperatures are 60 ℃ and 100 ℃ when the contents of diffusible hydrogen in the weld metal are 1ml / 100g and 2ml / 100g respectively .
试验结果表明,在焊缝金属扩散氢含量为1ml/100g和2ml/100g时,斜Y型铁研试验临界预热温度分别为60℃和100℃。
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100 Wistar rats were randomly divided into operation group with 85 infused bleomycin ( 1ml / kg ) through tracheal intubation and fake operation group with 15 rats infused normal saline of the same volum .
Wistar大鼠100只,随机分入手术组85只,气管插管灌注博莱霉素A5-生理盐水1mg/kg体重,假手术组15只,灌注等体积生理盐水。
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Through orthogonal experiment , the optimal extraction conditions were obtained as following : the volume ratio of two phases is 4:1 , the dilute times of soybean slurry is 3 times , the current velocity of soybean slurry is 1ml / min.
考察了流速、进料比等影响因素对萃取率的影响,通过正交实验确定了最佳的提取条件:两相(乙酸乙酯:大豆糖浆)进料比4:1,原料稀释倍数3,原料进料速度1ml/min。
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Normal saline was injected through the needle with the flow rate 1ml / s , 2ml / s , 3ml / s , 4ml / s respectively , then the various flow speed and volume were observed .
分别以1ml/s、2ml/s、3ml/s、4ml/s的流率经带侧孔穿刺针注射生理盐水,观察穿刺针各针孔流量的变化。
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Results ( 1 ) adding proper autologous blood (< 1ml ) to the preparation of bone cement ( 20g : 10ml ), there was not statistically significant among the hardness and other tested parameters except . the dough time .
结果:(1)所测参数中除面团时间外,以适量的自体血(1ml)配制骨水泥(20g:10ml)所得标本,其硬度等参数指标无统计学差异。
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Methods After anesthesia , myocardial contrast echocardiography ( MCE ) was performed on 10 closed chest dogs by peripheral intravenous injection of Sigma contrast agent ( 1ml / kg ) . Meanwhile , the heart rate and blood pressure were recorded .
方法10只闭胸狗麻醉后经周围静脉注射Sigma造影剂(1ml/kg)行心肌声学造影(MCE),同时观察其对实验犬心率、血压的影响。
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Before two hours of administration with TAA , each rat in group A and group B were given normal saline 1ml / 100g weight , and the left were given the same volume / weight medicine respectively , then redone every 8h .
在TAA首次造模前2h,A、B组每只大鼠灌胃生理盐水1ml/100g体重,其余各组给等体积/重量比的相应药物。以后每8h重复给药一次。